Tungsten-Mediated Decarboxylative C(sp <sup>3</sup> )–O Bond Formation through Ligand-to-Metal Charge Transfer

)-O bond formation reaction under mild, base-free conditions with irradiation. This transformation employs readily available carboxylic acids as substrates and 2,2,6,6-tetramethylpiperidin-1-oxyl (TEMPO) as oxygenation reagent. The protocol exhibits a broad substrate scope and has been successfully applied to the late-stage functionalization of bioactive molecules.

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Publication Details

Journal
The Journal of Organic Chemistry
Published
2026-04-17
DOI
https://doi.org/10.1021/acs.joc.6c00328
Primary Topic
Radical Photochemical Reactions
Type
article
Field-Weighted Citation Impact
0.00

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article

Tungsten-Mediated Decarboxylative C(sp 3 )–O Bond Formation through Ligand-to-Metal Charge Transfer

Heng Song, Shu-Fen Hou, Chen Xu, P. Bai et al.
The Journal of Organic Chemistry
Radical Photochemical Reactions
article

Tungsten-Mediated Decarboxylative C(sp 3 )–O Bond Formation through Ligand-to-Metal Charge Transfer

Heng Song, Shu-Fen Hou, Chen Xu, P. Bai, Siyu He, Yi Huang
article en

Abstract

)-O bond formation reaction under mild, base-free conditions with irradiation. This transformation employs readily available carboxylic acids as substrates and 2,2,6,6-tetramethylpiperidin-1-oxyl (TEMPO) as oxygenation reagent. The protocol exhibits a broad substrate scope and has been successfully applied to the late-stage functionalization of bioactive molecules.

The Journal of Organic ChemistryVol. 91(17)
Jiangsu University of Science and Technology (CN), Weifang University (CN)
National Natural Science Foundation of China, Natural Science Foundation of Shandong Province, Science and Technology Bureau of Zhenjiang
Openalex Percentile: Top 23%
Radical Photochemical Reactions
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